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Journal Abstract Search

212 related items for PubMed ID: 16999847

  • 21.
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  • 22. Molecular basis of fibrinogen deficiency.
    Neerman-Arbez M.
    Pathophysiol Haemost Thromb; 2006; 35(1-2):187-98. PubMed ID: 16855369
    [Abstract] [Full Text] [Related]

  • 23. Molecular basis of quantitative fibrinogen disorders in 27 patients from India.
    Sumitha E, Jayandharan GR, Arora N, Abraham A, David S, Devi GS, Shenbagapriya P, Nair SC, George B, Mathews V, Chandy M, Viswabandya A, Srivastava A.
    Haemophilia; 2013 Jul; 19(4):611-8. PubMed ID: 23560673
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  • 24. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
    Neerman-Arbez M, de Moerloose P.
    Hum Mutat; 2007 Jun; 28(6):540-53. PubMed ID: 17295221
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  • 27. Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient.
    Platé M, Asselta R, Peyvandi F, Tenchini ML, Duga S.
    Biochim Biophys Acta; 2007 Jul; 1772(7):781-7. PubMed ID: 17531448
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  • 28. Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
    Nojehdeh ST, Mojbafan M, Masoodifard M, Amini M, Zeinali S.
    Blood Coagul Fibrinolysis; 2021 Jul 01; 32(5):323-327. PubMed ID: 33901106
    [Abstract] [Full Text] [Related]

  • 29. Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.
    Spena S, Duga S, Asselta R, Peyvandi F, Mahasandana C, Malcovati M, Tenchini ML.
    Eur J Hum Genet; 2004 Nov 01; 12(11):891-8. PubMed ID: 15489905
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  • 32. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M, Leinoe E, Rossing M, Norström E, Zetterberg E.
    Blood Coagul Fibrinolysis; 2020 Oct 01; 31(7):481-484. PubMed ID: 32852326
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  • 35. Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites.
    Spena S, Duga S, Asselta R, Malcovati M, Peyvandi F, Tenchini ML.
    Blood; 2002 Dec 15; 100(13):4478-84. PubMed ID: 12393540
    [Abstract] [Full Text] [Related]

  • 36. Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia.
    Simurda T, Zolkova J, Kolkova Z, Loderer D, Dobrotova M, Skornova I, Brunclíkova M, Grendar M, Lasabova Z, Stasko J, Kubisz P.
    Int J Hematol; 2020 Jun 15; 111(6):795-802. PubMed ID: 32166693
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  • 38. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
    Castaman G, Rimoldi V, Giacomelli SH, Duga S.
    Thromb Res; 2015 Jul 15; 136(1):144-7. PubMed ID: 25981141
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